Loading…

Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes

Background We investigated the impact of depression and inflammatory markers, assessed 2 months after acute coronary syndrome (ACS), on major adverse cardiac events over 2 years (MACEs; cardiac death, survived myocardial infarction, survived cardiac arrest, and nonelective revascularization). Method...

Full description

Saved in:
Bibliographic Details
Published in:Biological psychiatry (1969) 2007-08, Vol.62 (4), p.302-308
Main Authors: Frasure-Smith, Nancy, Lespérance, François, Irwin, Michael R, Sauvé, Claude, Lespérance, Jacques, Théroux, Pierre
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43
cites cdi_FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43
container_end_page 308
container_issue 4
container_start_page 302
container_title Biological psychiatry (1969)
container_volume 62
creator Frasure-Smith, Nancy
Lespérance, François
Irwin, Michael R
Sauvé, Claude
Lespérance, Jacques
Théroux, Pierre
description Background We investigated the impact of depression and inflammatory markers, assessed 2 months after acute coronary syndrome (ACS), on major adverse cardiac events over 2 years (MACEs; cardiac death, survived myocardial infarction, survived cardiac arrest, and nonelective revascularization). Methods Depression symptoms (Beck Depression Inventory-II; BDI-II), major depression, C-reactive protein (CRP), interleukin-6, and soluble intercellular adhesion molecule were assessed in 741 ACS patients (including 602 men). Results Some 102 (78 men) experienced at least one MACE. Beck Depression Inventory-II scores of ≥14 predicted MACEs ( p = .007). The increase in risk was marked in men (hazard ratio [HR] = 1.96, 95% confidence interval [CI] = 1.24–3.09, p = .004), with little evidence of a relationship in women ( p = .85). Subsequent analyses were limited to men. Results were similar after covariate adjustment (HR = 1.72, 95% CI = 1.07–2.77, p = .024). C-reactive protein levels were also associated with increased MACE risk (adjusted HR for CRP ≥ 2.0 mg/L = 1.67, 95% CI = 1.07–2.62, p = .025). C-reactive protein levels and BDI-II scores interacted in predicting MACEs. Men with both BDI-II scores of ≥14 and CRP of ≥2.0 mg/L experienced an increase in risk similar to those with only one of these factors. Conclusions In men assessed 2 months after ACS, depression and CRP are overlapping prognostic risks. Patients with either risk may benefit from similar therapies.
doi_str_mv 10.1016/j.biopsych.2006.09.029
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68127039</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0006322306012169</els_id><sourcerecordid>20667514</sourcerecordid><originalsourceid>FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43</originalsourceid><addsrcrecordid>eNqFksFu1DAQhi0EokvhFSpf4ESCPUmc-IKolrYgtQKp5Wx57Ylw2LUXO1mUt8fRLqrEpb7Yo_nmH9v_EHLBWckZFx-GcuPCPs3mZwmMiZLJkoF8Rla8a6sCagbPyYrlTFEBVGfkVUpDDlsA_pKc8RaySs1WxH_GfcSUXPDv6bqIqM3oDki_xzCi81R7Sx_-hGJGHemdHkKkl_aAMSFd62idNvTqgH5MNMN3mAv6ETNjpjETIQav40zvZ29j2GF6TV70epvwzWk_Jz-urx7WX4rbbzdf15e3hWnqbiywtm1dQdda0yLLZxCNlLaqraia3tRgclZqu8lL9sZYiR1aAwzlBqCvq3Py7qi7j-H3hGlUO5cMbrfaY5iSEh2HllXySRCYEG3DF0VxBE0MKUXs1T66XX6c4kwtlqhB_bNELZYoJlW2JBdenDpMmx3ax7KTBxl4ewJ0MnrbR-2NS49cJzvRNZC5T0cO88cdHEaVjENv0LqIZlQ2uKfv8vE_CbN13uWuv3DGNIQp-myL4iqBYup-GaBlfphgHLiQ1V9uVcLe</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20667514</pqid></control><display><type>article</type><title>Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes</title><source>Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)</source><creator>Frasure-Smith, Nancy ; Lespérance, François ; Irwin, Michael R ; Sauvé, Claude ; Lespérance, Jacques ; Théroux, Pierre</creator><creatorcontrib>Frasure-Smith, Nancy ; Lespérance, François ; Irwin, Michael R ; Sauvé, Claude ; Lespérance, Jacques ; Théroux, Pierre</creatorcontrib><description>Background We investigated the impact of depression and inflammatory markers, assessed 2 months after acute coronary syndrome (ACS), on major adverse cardiac events over 2 years (MACEs; cardiac death, survived myocardial infarction, survived cardiac arrest, and nonelective revascularization). Methods Depression symptoms (Beck Depression Inventory-II; BDI-II), major depression, C-reactive protein (CRP), interleukin-6, and soluble intercellular adhesion molecule were assessed in 741 ACS patients (including 602 men). Results Some 102 (78 men) experienced at least one MACE. Beck Depression Inventory-II scores of ≥14 predicted MACEs ( p = .007). The increase in risk was marked in men (hazard ratio [HR] = 1.96, 95% confidence interval [CI] = 1.24–3.09, p = .004), with little evidence of a relationship in women ( p = .85). Subsequent analyses were limited to men. Results were similar after covariate adjustment (HR = 1.72, 95% CI = 1.07–2.77, p = .024). C-reactive protein levels were also associated with increased MACE risk (adjusted HR for CRP ≥ 2.0 mg/L = 1.67, 95% CI = 1.07–2.62, p = .025). C-reactive protein levels and BDI-II scores interacted in predicting MACEs. Men with both BDI-II scores of ≥14 and CRP of ≥2.0 mg/L experienced an increase in risk similar to those with only one of these factors. Conclusions In men assessed 2 months after ACS, depression and CRP are overlapping prognostic risks. Patients with either risk may benefit from similar therapies.</description><identifier>ISSN: 0006-3223</identifier><identifier>EISSN: 1873-2402</identifier><identifier>DOI: 10.1016/j.biopsych.2006.09.029</identifier><identifier>PMID: 17210140</identifier><identifier>CODEN: BIPCBF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Adult and adolescent clinical studies ; Aged ; Aged, 80 and over ; Angina, Unstable - blood ; Angina, Unstable - immunology ; Angina, Unstable - psychology ; Biological and medical sciences ; Biomarkers - blood ; C-Reactive Protein - analysis ; Cardiology. Vascular system ; Chi-Square Distribution ; Coronary heart disease ; CRP ; Depression ; depressive disorder ; Depressive Disorder - blood ; Depressive Disorder - complications ; Depressive Disorder - immunology ; Female ; Follow-Up Studies ; Heart ; Humans ; inflammation ; Inflammation Mediators - blood ; Interleukin-6 - blood ; Male ; Medical sciences ; Middle Aged ; Mood disorders ; myocardial infarction ; Myocardial Infarction - blood ; Myocardial Infarction - immunology ; Myocardial Infarction - psychology ; Myocarditis. Cardiomyopathies ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Risk Factors ; Sex Factors</subject><ispartof>Biological psychiatry (1969), 2007-08, Vol.62 (4), p.302-308</ispartof><rights>Society of Biological Psychiatry</rights><rights>2007 Society of Biological Psychiatry</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43</citedby><cites>FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18986852$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17210140$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frasure-Smith, Nancy</creatorcontrib><creatorcontrib>Lespérance, François</creatorcontrib><creatorcontrib>Irwin, Michael R</creatorcontrib><creatorcontrib>Sauvé, Claude</creatorcontrib><creatorcontrib>Lespérance, Jacques</creatorcontrib><creatorcontrib>Théroux, Pierre</creatorcontrib><title>Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes</title><title>Biological psychiatry (1969)</title><addtitle>Biol Psychiatry</addtitle><description>Background We investigated the impact of depression and inflammatory markers, assessed 2 months after acute coronary syndrome (ACS), on major adverse cardiac events over 2 years (MACEs; cardiac death, survived myocardial infarction, survived cardiac arrest, and nonelective revascularization). Methods Depression symptoms (Beck Depression Inventory-II; BDI-II), major depression, C-reactive protein (CRP), interleukin-6, and soluble intercellular adhesion molecule were assessed in 741 ACS patients (including 602 men). Results Some 102 (78 men) experienced at least one MACE. Beck Depression Inventory-II scores of ≥14 predicted MACEs ( p = .007). The increase in risk was marked in men (hazard ratio [HR] = 1.96, 95% confidence interval [CI] = 1.24–3.09, p = .004), with little evidence of a relationship in women ( p = .85). Subsequent analyses were limited to men. Results were similar after covariate adjustment (HR = 1.72, 95% CI = 1.07–2.77, p = .024). C-reactive protein levels were also associated with increased MACE risk (adjusted HR for CRP ≥ 2.0 mg/L = 1.67, 95% CI = 1.07–2.62, p = .025). C-reactive protein levels and BDI-II scores interacted in predicting MACEs. Men with both BDI-II scores of ≥14 and CRP of ≥2.0 mg/L experienced an increase in risk similar to those with only one of these factors. Conclusions In men assessed 2 months after ACS, depression and CRP are overlapping prognostic risks. Patients with either risk may benefit from similar therapies.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Angina, Unstable - blood</subject><subject>Angina, Unstable - immunology</subject><subject>Angina, Unstable - psychology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>C-Reactive Protein - analysis</subject><subject>Cardiology. Vascular system</subject><subject>Chi-Square Distribution</subject><subject>Coronary heart disease</subject><subject>CRP</subject><subject>Depression</subject><subject>depressive disorder</subject><subject>Depressive Disorder - blood</subject><subject>Depressive Disorder - complications</subject><subject>Depressive Disorder - immunology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Heart</subject><subject>Humans</subject><subject>inflammation</subject><subject>Inflammation Mediators - blood</subject><subject>Interleukin-6 - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mood disorders</subject><subject>myocardial infarction</subject><subject>Myocardial Infarction - blood</subject><subject>Myocardial Infarction - immunology</subject><subject>Myocardial Infarction - psychology</subject><subject>Myocarditis. Cardiomyopathies</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><issn>0006-3223</issn><issn>1873-2402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFksFu1DAQhi0EokvhFSpf4ESCPUmc-IKolrYgtQKp5Wx57Ylw2LUXO1mUt8fRLqrEpb7Yo_nmH9v_EHLBWckZFx-GcuPCPs3mZwmMiZLJkoF8Rla8a6sCagbPyYrlTFEBVGfkVUpDDlsA_pKc8RaySs1WxH_GfcSUXPDv6bqIqM3oDki_xzCi81R7Sx_-hGJGHemdHkKkl_aAMSFd62idNvTqgH5MNMN3mAv6ETNjpjETIQav40zvZ29j2GF6TV70epvwzWk_Jz-urx7WX4rbbzdf15e3hWnqbiywtm1dQdda0yLLZxCNlLaqraia3tRgclZqu8lL9sZYiR1aAwzlBqCvq3Py7qi7j-H3hGlUO5cMbrfaY5iSEh2HllXySRCYEG3DF0VxBE0MKUXs1T66XX6c4kwtlqhB_bNELZYoJlW2JBdenDpMmx3ax7KTBxl4ewJ0MnrbR-2NS49cJzvRNZC5T0cO88cdHEaVjENv0LqIZlQ2uKfv8vE_CbN13uWuv3DGNIQp-myL4iqBYup-GaBlfphgHLiQ1V9uVcLe</recordid><startdate>20070815</startdate><enddate>20070815</enddate><creator>Frasure-Smith, Nancy</creator><creator>Lespérance, François</creator><creator>Irwin, Michael R</creator><creator>Sauvé, Claude</creator><creator>Lespérance, Jacques</creator><creator>Théroux, Pierre</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20070815</creationdate><title>Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes</title><author>Frasure-Smith, Nancy ; Lespérance, François ; Irwin, Michael R ; Sauvé, Claude ; Lespérance, Jacques ; Théroux, Pierre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Angina, Unstable - blood</topic><topic>Angina, Unstable - immunology</topic><topic>Angina, Unstable - psychology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>C-Reactive Protein - analysis</topic><topic>Cardiology. Vascular system</topic><topic>Chi-Square Distribution</topic><topic>Coronary heart disease</topic><topic>CRP</topic><topic>Depression</topic><topic>depressive disorder</topic><topic>Depressive Disorder - blood</topic><topic>Depressive Disorder - complications</topic><topic>Depressive Disorder - immunology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Heart</topic><topic>Humans</topic><topic>inflammation</topic><topic>Inflammation Mediators - blood</topic><topic>Interleukin-6 - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mood disorders</topic><topic>myocardial infarction</topic><topic>Myocardial Infarction - blood</topic><topic>Myocardial Infarction - immunology</topic><topic>Myocardial Infarction - psychology</topic><topic>Myocarditis. Cardiomyopathies</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frasure-Smith, Nancy</creatorcontrib><creatorcontrib>Lespérance, François</creatorcontrib><creatorcontrib>Irwin, Michael R</creatorcontrib><creatorcontrib>Sauvé, Claude</creatorcontrib><creatorcontrib>Lespérance, Jacques</creatorcontrib><creatorcontrib>Théroux, Pierre</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frasure-Smith, Nancy</au><au>Lespérance, François</au><au>Irwin, Michael R</au><au>Sauvé, Claude</au><au>Lespérance, Jacques</au><au>Théroux, Pierre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>2007-08-15</date><risdate>2007</risdate><volume>62</volume><issue>4</issue><spage>302</spage><epage>308</epage><pages>302-308</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>Background We investigated the impact of depression and inflammatory markers, assessed 2 months after acute coronary syndrome (ACS), on major adverse cardiac events over 2 years (MACEs; cardiac death, survived myocardial infarction, survived cardiac arrest, and nonelective revascularization). Methods Depression symptoms (Beck Depression Inventory-II; BDI-II), major depression, C-reactive protein (CRP), interleukin-6, and soluble intercellular adhesion molecule were assessed in 741 ACS patients (including 602 men). Results Some 102 (78 men) experienced at least one MACE. Beck Depression Inventory-II scores of ≥14 predicted MACEs ( p = .007). The increase in risk was marked in men (hazard ratio [HR] = 1.96, 95% confidence interval [CI] = 1.24–3.09, p = .004), with little evidence of a relationship in women ( p = .85). Subsequent analyses were limited to men. Results were similar after covariate adjustment (HR = 1.72, 95% CI = 1.07–2.77, p = .024). C-reactive protein levels were also associated with increased MACE risk (adjusted HR for CRP ≥ 2.0 mg/L = 1.67, 95% CI = 1.07–2.62, p = .025). C-reactive protein levels and BDI-II scores interacted in predicting MACEs. Men with both BDI-II scores of ≥14 and CRP of ≥2.0 mg/L experienced an increase in risk similar to those with only one of these factors. Conclusions In men assessed 2 months after ACS, depression and CRP are overlapping prognostic risks. Patients with either risk may benefit from similar therapies.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17210140</pmid><doi>10.1016/j.biopsych.2006.09.029</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-3223
ispartof Biological psychiatry (1969), 2007-08, Vol.62 (4), p.302-308
issn 0006-3223
1873-2402
language eng
recordid cdi_proquest_miscellaneous_68127039
source Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)
subjects Adult
Adult and adolescent clinical studies
Aged
Aged, 80 and over
Angina, Unstable - blood
Angina, Unstable - immunology
Angina, Unstable - psychology
Biological and medical sciences
Biomarkers - blood
C-Reactive Protein - analysis
Cardiology. Vascular system
Chi-Square Distribution
Coronary heart disease
CRP
Depression
depressive disorder
Depressive Disorder - blood
Depressive Disorder - complications
Depressive Disorder - immunology
Female
Follow-Up Studies
Heart
Humans
inflammation
Inflammation Mediators - blood
Interleukin-6 - blood
Male
Medical sciences
Middle Aged
Mood disorders
myocardial infarction
Myocardial Infarction - blood
Myocardial Infarction - immunology
Myocardial Infarction - psychology
Myocarditis. Cardiomyopathies
Prognosis
Proportional Hazards Models
Prospective Studies
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Risk Factors
Sex Factors
title Depression, C-reactive Protein and Two-year Major Adverse Cardiac Events in Men after Acute Coronary Syndromes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T01%3A14%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Depression,%20C-reactive%20Protein%20and%20Two-year%20Major%20Adverse%20Cardiac%20Events%20in%20Men%20after%20Acute%20Coronary%20Syndromes&rft.jtitle=Biological%20psychiatry%20(1969)&rft.au=Frasure-Smith,%20Nancy&rft.date=2007-08-15&rft.volume=62&rft.issue=4&rft.spage=302&rft.epage=308&rft.pages=302-308&rft.issn=0006-3223&rft.eissn=1873-2402&rft.coden=BIPCBF&rft_id=info:doi/10.1016/j.biopsych.2006.09.029&rft_dat=%3Cproquest_cross%3E20667514%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c548t-e4d743287dc7e0d7426599d34d635fc42c4329adbbbb9fccd9e8edc20e9b22f43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20667514&rft_id=info:pmid/17210140&rfr_iscdi=true